Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tom Bohling"'
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-9 (2017)
Abstract Background Distinct characteristic features categorize Merkel cell carcinoma (MCC) into two subgroups according to the Merkel cell polyomavirus infection. Many mutational studies on MCC have been carried out in recent years without identifyi
Externí odkaz:
https://doaj.org/article/61b42dc0999c4da0b90d60ad7ffeba68
Autor:
Nebeyu Y. Gizaw, Pauliina Kallio, Erika Gucciardo, Caj Haglund, Tom Bohling, Kaisa Lehti, Mika Sampo, Kari Alitalo, Riikka Kivela
Publikováno v:
Clinical Cancer Research. 28:A026-A026
Rhabdomyosarcoma (RMS) is an aggressive pediatric soft tissue cancer with features of skeletal muscle. Because of poor survival of RMS patients and severe long-term side effects of RMS therapies, novel RMS therapies are urgently needed. Here we show
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55071c4027bd1f00c550cbcb91640fe1
https://doi.org/10.1158/1557-3265.sarcomas22-a026
https://doi.org/10.1158/1557-3265.sarcomas22-a026
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Eccrine porocarcinoma (EPC) is a rare malignant adnexal tumour of the skin. Part of EPCs develop from their benign counterpart, poroma (EP), with chronic light exposure and immunosuppression hypothesized to play a role in the malignant trans
Externí odkaz:
https://doaj.org/article/99dd7dc725934cc18ee3063005cac510
Autor:
Marko Salmikangas, Maria Laaksonen, Henrik Edgren, Marco Salgado, Anu Suoranta, Pirkko Mattila, Virve Koljonen, Tom Böhling, Harri Sihto
Publikováno v:
PLoS ONE, Vol 18, Iss 5, p e0285524 (2023)
Merkel cell carcinoma (MCC) is a rare cutaneous neuroendocrine carcinoma that is frequently divided into Merkel cell polyomavirus negative and positive tumors due their distinct genomic and transcriptomic profiles, and disease outcomes. Although some
Externí odkaz:
https://doaj.org/article/b73c83bccbc64b178f32e9e4e9d24760
Autor:
Klaus W Fagerstedt, Tom Böhling, Harri Sihto, Tarja Salonen, Fang Zhao, Mia Kero, Leif C Andersson, Johanna Arola
Publikováno v:
Endocrine Connections, Vol 10, Iss 9, Pp 1055-1064 (2021)
Mixed neuroendocrine-non-neuroendocrine neoplasms (MINEN) are rare tumors that consist of at least 30% of both neuroendocrine and non-neuroendocrine components. The data concerning the pathogenesis of MINEN suggest a monoclonal origin. We describe a
Externí odkaz:
https://doaj.org/article/baa7f4ad70af4838bd6c0143f8f71647
Autor:
Eeva Kettunen, Sauli Savukoski, Kaisa Salmenkivi, Tom Böhling, Esa Vanhala, Eeva Kuosma, Sisko Anttila, Henrik Wolff
Publikováno v:
BMC Cancer, Vol 19, Iss 1, Pp 1-10 (2019)
Abstract Background Deletion of the CDKN2A locus is centrally involved in the development of several malignancies. In malignant pleural mesothelioma (MPM), it is one of the most frequently reported genomic alteration. MPM is strongly associated with
Externí odkaz:
https://doaj.org/article/131cca9545364481bce20e538437397f
Publikováno v:
PLoS ONE, Vol 16, Iss 5, p e0252099 (2021)
Merkel cell carcinoma (MCC) is a rare skin cancer with only limited therapeutic options for advanced disease. We previously showed that oncogene ALK is frequently expressed at the RNA level in MCC and further that ALK positivity by immunohistochemist
Externí odkaz:
https://doaj.org/article/1ba0b773467f4185a9e5fb91ca628588
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 1, p adv00363 (2021)
Malignant eccrine porocarcinoma is a rare skin adnexal cancer arising from the sweat glands. Little is known about the epidemiology and incidence of eccrine porocarcinoma. This registry-based study examined the epidemiology and incidence data for ecc
Externí odkaz:
https://doaj.org/article/866ba9e184b8421095eadb1bd5c6aab9
Publikováno v:
Tumor Biology, Vol 40 (2018)
Myxoinflammatory fibroblastic sarcoma is a soft-tissue neoplasm most frequently found in the distal extremities of middle-aged adults. Most myxoinflammatory fibroblastic sarcoma are low-grade tumors with propensity for local recurrence after incomple
Externí odkaz:
https://doaj.org/article/1e1ff3433e4343cca40dcbdc2b173890